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Degradation and translation of maternal mRNA for embryogenesis.
Yang, Guanghui; Xin, Qiliang; Dean, Jurrien.
Afiliación
  • Yang G; Laboratory of Cellular and Developmental Biology, NIDDK, National Institutes of Health, Bethesda, MD 20892, USA. Electronic address: guanghui.yang@nih.gov.
  • Xin Q; Laboratory of Cellular and Developmental Biology, NIDDK, National Institutes of Health, Bethesda, MD 20892, USA.
  • Dean J; Laboratory of Cellular and Developmental Biology, NIDDK, National Institutes of Health, Bethesda, MD 20892, USA. Electronic address: jurrien.dean@nih.gov.
Trends Genet ; 40(3): 238-249, 2024 03.
Article en En | MEDLINE | ID: mdl-38262796
ABSTRACT
Maternal mRNAs accumulate during egg growth and must be judiciously degraded or translated to ensure successful development of mammalian embryos. In this review we integrate recent investigations into pathways controlling rapid degradation of maternal mRNAs during the maternal-to-zygotic transition. Degradation is not indiscriminate, and some mRNAs are selectively protected and rapidly translated after fertilization for reprogramming the zygotic genome during early embryogenesis. Oocyte specific cofactors and pathways have been illustrated to control different futures of maternal mRNAs. We discuss mechanisms that control the fate of maternal mRNAs during late oogenesis and after fertilization. Issues to be resolved in current maternal mRNA research are described, and future research directions are proposed.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: ARN Mensajero Almacenado / Desarrollo Embrionario Límite: Animals Idioma: En Revista: Trends Genet Asunto de la revista: GENETICA Año: 2024 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: ARN Mensajero Almacenado / Desarrollo Embrionario Límite: Animals Idioma: En Revista: Trends Genet Asunto de la revista: GENETICA Año: 2024 Tipo del documento: Article